TY - JOUR
T1 - Bilateral common carotid artery ligation transiently changes brain lipid metabolism in rats
AU - Bhattacharjee, Abesh Kumar
AU - White, Laura
AU - Chang, Lisa
AU - Ma, Kaizong
AU - Harry, G. Jean
AU - Deutsch, Joseph
AU - Rapoport, Stanley I.
PY - 2012/7
Y1 - 2012/7
N2 - Brain lipid metabolism was studied in rats following permanent bilateral common carotid artery ligation (BCCL), a model for chronic cerebral hypoperfusion. Unesterified (free) fatty acids (uFA) and acyl-CoA concentrations were measured 6 h, 24 h, and 7 days after BCCL or sham surgery, in high energy-microwaved brain. In BCCL compared to sham rats, cytosolic phospholipase A2 (cPLA2) immunoreactivity in piriform cortex, and concentrations of total uFA and arachidonoyl-CoA, an intermediate for arachidonic acid reincorporation into phospholipids, were increased only at 6 h. At 24 h, immunoreactivity for secretory phospholipase A2 (sPLA2), which may regulate blood flow, was increased near cortical and hippocampal blood vessels. BCCL did not affect levels of brain IB4+ microglia, glial fibrillary acidic protein (GFAP) astrocytes, cyclooxygenase-2 (COX-2) immunoreactivity at any time, but increased cPLA2 immunoreactivity in one region at 6 h. Thus, BCCL affected brain lipid metabolism transiently, likely because of compensatory sPLA2-mediated vasodilation, without producing evidence of neuroinflammation.
AB - Brain lipid metabolism was studied in rats following permanent bilateral common carotid artery ligation (BCCL), a model for chronic cerebral hypoperfusion. Unesterified (free) fatty acids (uFA) and acyl-CoA concentrations were measured 6 h, 24 h, and 7 days after BCCL or sham surgery, in high energy-microwaved brain. In BCCL compared to sham rats, cytosolic phospholipase A2 (cPLA2) immunoreactivity in piriform cortex, and concentrations of total uFA and arachidonoyl-CoA, an intermediate for arachidonic acid reincorporation into phospholipids, were increased only at 6 h. At 24 h, immunoreactivity for secretory phospholipase A2 (sPLA2), which may regulate blood flow, was increased near cortical and hippocampal blood vessels. BCCL did not affect levels of brain IB4+ microglia, glial fibrillary acidic protein (GFAP) astrocytes, cyclooxygenase-2 (COX-2) immunoreactivity at any time, but increased cPLA2 immunoreactivity in one region at 6 h. Thus, BCCL affected brain lipid metabolism transiently, likely because of compensatory sPLA2-mediated vasodilation, without producing evidence of neuroinflammation.
KW - Acyl-CoA
KW - Arachidonic acid
KW - Brain
KW - Carotid
KW - CPLA2
KW - Ischemia
KW - Ligation
KW - Rat Brain Neuroinflammation
KW - SPLA2
UR - http://www.scopus.com/inward/record.url?scp=84862889559&partnerID=8YFLogxK
U2 - 10.1007/s11064-012-0740-2
DO - 10.1007/s11064-012-0740-2
M3 - ???researchoutput.researchoutputtypes.contributiontojournal.article???
C2 - 22422289
AN - SCOPUS:84862889559
SN - 0364-3190
VL - 37
SP - 1490
EP - 1498
JO - Neurochemical Research
JF - Neurochemical Research
IS - 7
ER -